Cleared Special

K992277 - STAPLETAC BONE ANCHOR SYSTEM

K992277 is an FDA 510(k) clearance for STAPLETAC BONE ANCHOR SYSTEM, manufactured by Influence, Inc.. The device is a Class 2 Orthopedic device with product code HWC cleared through the Special 510(k) pathway after a 23-day FDA review.

K992277 · Influence, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1999
Decision
23d
Days
Class 2
Risk

K992277 is an FDA 510(k) clearance for the STAPLETAC BONE ANCHOR SYSTEM. Classified as Screw, Fixation, Bone (product code HWC), Class II - Special Controls.

Submitted by Influence, Inc. (Washington, US). The FDA issued a Cleared decision on July 30, 1999 after a review of 23 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - the FDA orthopedic device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Influence, Inc. devices

FDA 510(k) Submission Details - K992277

510(k) Number K992277 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 07, 1999
Decision Date July 30, 1999
Days to Decision 23 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
99d faster than avg
Panel avg: 122d · This submission: 23d
Pathway characteristics
Modification to existing cleared device.

HWC Device Classification - Class 2, Special Controls

Product Code HWC Screw, Fixation, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - HWC Screw, Fixation, Bone

All 809
Devices cleared under the same product code (HWC) and FDA review panel - the closest regulatory comparables to K992277.
MODUS SYSTEM SELF-DRILLING SCREWS
K992106 · Medartis AG · Sep 1999
REUNITE SCREWS
K992301 · Biomet Manufacturing, Inc. · Sep 1999
BIORC ANCHOR
K990770 · Linvatec Corp. · Jul 1999
SPIN SNAP-OFF SCREW
K991477 · New Deal, S.A. · Jul 1999
BIO-INTERFERENCE SCREW
K990454 · Innovasive Devices, Inc. · Jul 1999
BONE SCREWS
K990351 · Bregma International Trading Company , Ltd. · Jun 1999